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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2E
(T94fs)
Deletion
(frameshift variant)
not provided
+1 more
GConflicting classifications of pathogenicity
KMT2E
(S1303*)
Single nucleotide variant
(nonsense)
O'Donnell-Luria-Rodan syndrome
GPathogenic
KMT2E
(H1446fs)
Microsatellite
(frameshift variant)
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies
GLikely pathogenic
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